field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
We are looking for a research scientist to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.
In this role you will need to hold an expert understanding of chemistry- a completed or in progress Masters/PhD is preferred but not required. Other related fields include, but are not limited to: Research and Development Chemist, Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist.
Benefits:
<ul>
<li>This is a full-time or part-time REMOTE position</li>
<li>You’ll be able to choose which projects you want to work on</li>
<li>You can work on your own schedule</li>
<li>Projects are paid hourly starting at $40+ per hour, with bonuses on high-quality and high-volume work</li>
</ul>
Responsibilities:
<ul>
<li>Give AI chatbots diverse and complex chemistry problems and evaluate their outputs</li>
<li>Evaluate the quality produced by AI models for correctness and performance</li>
</ul>
Qualifications:
<ul>
<li>A current, in progress, or completed Masters and/or PhD is preferred but not required</li>
<li>Fluency in English (native or bilingual level)</li>
<li>Detail-oriented</li>
<li>Proficient in chemistry, inductive/deductive reasoning, physical/temporal/ spatial reasoning</li>
</ul>
Note: Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. This job is only available to those in the US, UK, Canada, Australia, or New Zealand. Those located outside of these countries will not see work or assessments available on our site at this time.

Chemical Technician

Senior Chemist

Quality Control Chemist

<h3>Job Description</h3>
Job Description
Akkodis is seeking a Research Associate for a Contract job with a client in Waltham, MA. Responsibilities include implementing molecular biology techniques and collaborating on in vitro and in vivo screening studies.
Rate Range: $50/hour to $55/hour; The rate may be negotiable based on experience, education, geographic location, and other factors.
Research Associate job responsibilities include:
<ul>
<li>
Support and execute NGS workflows, including amplicon sequencing and RNA-seq for in vitro and in vivo studies.
</li>
<li>
Operate and maintain sequencing instruments, such as Illumina NextSeq, ensuring high-quality data output.
</li>
<li>
Collaborate with cross-functional teams to process samples and implement molecular biology and biochemistry techniques.
</li>
<li>
Maintain accurate experimental records and perform data analysis using NGS platforms.
</li>
<li>
Present findings in internal meetings and contribute to experimental design and troubleshooting.
</li>
<li>
Manage lab automation tools and ensure adherence to quality control procedures and timelines.
</li>
</ul>
Desired Qualifications:
<ul>
<li>
Bachelor’s or master’s degree in biotechnology, Molecular Biology, or a related field.
</li>
<li>
At least 2 years of hands-on experience with next-generation sequencing techniques.
</li>
<li>
Proficiency in RNA-seq and amplicon sequencing, with experience operating Illumina NextSeq instruments.
</li>
<li>
Familiarity with NGS data analysis platforms and laboratory automation tools for sequencing workflows.
</li>
</ul>
If you are interested in this role, then please click APPLY NOW. For other opportunities available at Akkodis, or any questions, feel free to contact me at Prakhar.Gupta@akkodisgroup.com
 Pay Details: $50.00 to $55.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to <a href="https://www.akkodis.com/en/us/candidate-privacy-policy" target="_blank">https://www.akkodis.com/en/us/candidate-privacy-policy</a> The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: 
<ul>
<li>The California Fair Chance Act</li>
<li>Los Angeles City Fair Chance Ordinance</li>
<li>Los Angeles County Fair Chance Ordinance for Employers</li>
<li>San Francisco Fair Chance Ordinance</li>
</ul>
 Company DescriptionGlobal Footprint, Local Impact: As part of the world's second-largest ER&amp;D company, you'll join a network of 50,000 professionals across 30 countries, each contributing to impactful projects worldwide while benefiting from a close-knit community at a local level. Diverse Career Paths: With services ranging from specialist recruitment to cloud infrastructure and sustainability, Akkodis offers a multitude of career paths. Whether you're a software developer, data analyst, or sustainability expert, there's a place for your skill set. Commitment to Innovation: Innovation is our cornerstone. With continuous investments in analytics and market intelligence, we not only predict the future of technology – we create it. Your ideas and innovations will have the space to flourish. Continuous Learning and Development: The Akkodis Academy offers unrivaled opportunities for learning and professional growth, ensuring you remain at the forefront of your field. Our culture values continuous improvement, both for our company and for your career. Inclusive and Collaborative Culture: We believe in the power of diverse perspectives and collaborative work environments. At Akkodis, you'll find a community where inclusivity drives innovation and where every voice is heard. Our Evolution and Your Role in It Akkodis emerged from the strategic merger of AKKA Technologies and Modis in 2023, under the Adecco Group. This fusion created a powerhouse in digital engineering and technology, blending European engineering finesse with global technological capabilities. As we write our next chapter, your skills and vision will be instrumental in driving our continued success. Empowering the Future We're not just creating solutions; we're empowering industries to be more efficient, sustainable, and forward-thinking. Our work in industrial automation, product development, and custom software solutions is setting new standards in technology and engineering. Join the Akkodis Community At Akkodis, you're more than just an employee – you're a vital part of a community shaping the future. We're excited to see where your expertise can take us. Discover where you fit in our diverse range of opportunities and start engineering a smarter future with us today. 
<h3>Company Description</h3>
Global Footprint, Local Impact: As part of the world's second-largest ER&amp;D company, you'll join a network of 50,000 professionals across 30 countries, each contributing to impactful projects worldwide while benefiting from a close-knit community at a local level.\r\n\r\nDiverse Career Paths: With services ranging from specialist recruitment to cloud infrastructure and sustainability, Akkodis offers a multitude of career paths. Whether you're a software developer, data analyst, or sustainability expert, there's a place for your skill set.\r\n\r\nCommitment to Innovation: Innovation is our cornerstone. With continuous investments in analytics and market intelligence, we not only predict the future of technology – we create it. Your ideas and innovations will have the space to flourish.\r\n\r\nContinuous Learning and Development: The Akkodis Academy offers unrivaled opportunities for learning and professional growth, ensuring you remain at the forefront of your field. Our culture values continuous improvement, both for our company and for your career.\r\n\r\nInclusive and Collaborative Culture: We believe in the power of diverse perspectives and collaborative work environments. At Akkodis, you'll find a community where inclusivity drives innovation and where every voice is heard.\r\n\r\nOur Evolution and Your Role in It\r\n\r\nAkkodis emerged from the strategic merger of AKKA Technologies and Modis in 2023, under the Adecco Group. This fusion created a powerhouse in digital engineering and technology, blending European engineering finesse with global technological capabilities. As we write our next chapter, your skills and vision will be instrumental in driving our continued success.\r\n\r\nEmpowering the Future\r\n\r\nWe're not just creating solutions; we're empowering industries to be more efficient, sustainable, and forward-thinking. Our work in industrial automation, product development, and custom software solutions is setting new standards in technology and engineering.\r\n\r\nJoin the Akkodis Community\r\n\r\nAt Akkodis, you're more than just an employee – you're a vital part of a community shaping the future. We're excited to see where your expertise can take us. Discover where you fit in our diverse range of opportunities and start engineering a smarter future with us today.

Research Associate

<h3>Job Description</h3>
Job Description
This is a full-time 40 hour a week position. (Schedule is 4 days, 10 hour shifts) 
THE POSITION:
The Senior Microbiology Medical Technologist (MT) works in collaboration with the veterinary staff and the Pathology team to provide Angell clientele with high quality clinical and anatomical laboratory services. The Senior Microbiology MT will assist in the opening of the new, state of the art Microbiology laboratory. The Senior Microbiology MT will help set up the laboratory space and workflow, train on all new Microbiology analyzers, train laboratory employees on microbiology procedures, develop and modify existing and new procedures and protocols, establish and monitor QC programs and help oversee the microbiology laboratory when required by Management. The Senior Microbiology MT uses a variety of technical and analytical skills to perform and evaluate various laboratory test procedures to aid the doctors in the diagnosis, treatment and monitoring of patients to provide accurate and timely results. The Senior Microbiology MT will be cross trained into the Clinical Pathology laboratory as a generalist after becoming proficient in the microbiology laboratory. This position also requires collaboration and daily interaction with the clinical pathology laboratory. Working knowledge of current Microbiology practices, use of Maldi-Tof technology and the most updated CLSI and ASM guidelines is a preferred. Experience reading and evaluating all microbiology benches both human and veterinary is optimal.
Some of the duties include:
<ul>
<li>
<ul>
<li>Possesses and demonstrates technical and theoretical knowledge of clinical and veterinary Microbiology.</li>
<li>Responsible for reading all microbiology culture plates and processing all appropriate testing for those cultures.</li>
<li>Responsible for the training of new and current employees in the microbiology laboratory. Updates training protocols and procedures as needed. Accurately records, discusses and troubleshoots trainee’s progress with the supervisor and lab management. Provides timely feedback for all trainees to lab management as needed.</li>
<li>Performs clinical testing and complex analysis of biological materials. Testing includes analysis of not only patient specimens but also proficiency samples, quality control (QC) material and calibration of methods, equipment and instruments.</li>
<li>Evaluates patient test results to verify validity of results and identify and resolve any inconsistencies in patient results. Provides clinical expertise to the patient care staff with the interpretation of results and/or complex laboratory problems.</li>
<li>Operates, maintains, troubleshoots and resolves issues with laboratory instrumentation, equipment and test assays. Documents minor repairs and maintenance procedures. Consistently uses available resources to maintain and repair instruments or problem solves assay issues.</li>
</ul>
</li>
</ul>
WHO WE ARE:
The Boston MSPCA-Angell is one of the oldest and most venerable humane organizations in the world, and working in an environment that clearly delivers on its mission of advancing the health and welfare of animals adds an important dimension to our work.
APPLICANT REQUIREMENTS: 
Education: Graduate of NAACLs accredited Clinical Laboratory Science program with certification as a Medical Technologist (MT), Medical Laboratory Scientist (MLS), Clinical Laboratory Scientist (CLS) or Microbiology Specialist (M ASCP) by ASCP or other nationally recognized credentialing agency is required. Bachelor of Science in a medical discipline with 5+ years of veterinary or human microbiology bench reading experience will be considered.
Experience: 5+ years of current Microbiology bench reading experience is preferred. Both veterinary and human microbiology experience will be considered.
OUR BENEFITS:
Our compensation package includes health, dental and life insurance, 403(b) retirement plan, tuition reimbursement, paid holidays, sick, and vacation time, employee discounts for pet health care, and free on-site parking.
If you are interested in working for an organization where your work is an important part of a respected and caring non-profit, this may be the career change you are looking for.

Senior Microbiology Medical Technologist

<h3>Job Description</h3>
Job title: Global Scientific Communications Lead – Rare Disease
Location: Cambridge, MA
About the job
We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&amp;D to sales, our talented teams work together, revolutionizing treatment, continually improving products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.​
Associate Director, Global Rare Diseases Scientific Communications &amp; Publications, oversees the development and execution of the strategic publication and scientific communication plan for multiple indications including launched products and development indications in the Rare Franchise.
We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&amp;D to sales, our talented teams work together, revolutionizing treatment, continually improving products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.
Main Responsibilities:
The Scientific Communications Lead will closely collaborate with external thought leaders and internal stakeholders in the medical, scientific affairs, biostats and clinical development teams by leading:
<ul>
<li>
Strategic publication planning and execution: Overseeing the development of abstracts for medical and scientific congresses, posters, platform presentations, manuscripts, and journal publication enhancements.
</li>
<li>
Scientific communications strategic planning and resource development: Creating scientific platforms, lexicons, FAQs, and backgrounders, as well as supporting content development for advisory boards.
</li>
<li>
Medical education planning and execution: Developing content for live education programs, congress symposia, online and multichannel HCP education, field medical tools, slide decks, medical booth resources, and omnichannel engagement assets.
</li>
<li>
This role reports to the Director Global Scientific Communications for launch indications within Rare Diseases in Global Medical Affairs at Sanofi.
</li>
<li>
Collaboration with external authors and academic experts is essential to drive execution of high quality and relevant publications and medical education materials to address educational and data gaps and inform strategic decision making.
</li>
<li>
In addition to investigators/authors, a key element of this role involves managing scientific agencies and requires working closely with cross-functional teams and internal stakeholders, particularly from the Registry, Research and Clinical Development, to drive the data generation strategy and integration of scientific, clinical, and business priorities.
</li>
<li>
The Scientific Communications Lead will have experience and a proven track record of success in the biotechnology or pharmaceutical industry, with a strong background in scientific research, publication planning, medical communications, and medical affairs activities
</li>
</ul>
About You
Qualifications and Skills:
<ul>
<li>
Advance degree in life sciences or pharmaceutical sciences (PhD, PharmD, MD or MS) with 2+ years of relevant medical affairs experience.
</li>
<li>
A minimum of 2+ years pharma/biotech industry in a global role
</li>
<li>
Experience working in a matrix organization and across team is preferred.
</li>
<li>
Ability to interpret and critique scientific and medical data with respect to scientific and business implications are essential.
</li>
<li>
Experience and demonstrated skill in the analysis, communication, and presentation of complex scientific and medical data.
</li>
<li>
Track record of successfully developing peer-reviewed publications is required.
</li>
<li>
Exemplary customer facing skills, and ability to collaborate with external Key Opinion Leaders on data dissemination strategies in a credible, responsive and customer focused manner is a necessity.
</li>
<li>
Excellent interpersonal and communication skills, written and verbal; comfortable and experienced in making presentations.
</li>
<li>
Demonstrated ability to work effectively in a matrix environment.
</li>
<li>
Experience collaborating with and supporting international medical scientific teams.
</li>
<li>
Knowledge of industry guidelines pertaining to data dissemination (e.g., CONSORT, ICMJE, GPPs) and interactions with health care providers (e.g., PhRMA Code, AdvaMed guidelines)
</li>
</ul>
Why Choose Us?
<ul>
<li>
Bring the miracles of science to life alongside a supportive, future-focused team.
</li>
<li>
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
</li>
<li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
</li>
<li>
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
</li>
</ul>
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law
#GD-SG &nbsp;​ &nbsp;#LI-GZ
#LI-Onsite
#vhd
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Global Scientific Communications Lead - Rare Disease

<h3>Job Description</h3>
Job Description
We are seeking a motivated and skilled Research Assistant with a strong background in molecular biology and assay development to support our research team. The ideal candidate will have hands-on experience with cell culture, protein purification, and the development of molecular assays. This role is critical in helping to drive the early-stage research that underpins our core product development and will involve working closely with a small, interdisciplinary team of scientists and researchers.
Key Responsibilities:
<ul>
<li>Conduct molecular biology experiments, including DNA/RNA extraction, PCR, cloning, and gene expression analysis.</li>
<li>Develop and optimize assays to support ongoing research projects, ensuring high sensitivity, specificity, and reproducibility.</li>
<li>Maintain and troubleshoot mammalian and/or bacterial cell cultures, following sterile techniques and ensuring cell line viability and quality.</li>
<li>Perform protein expression and purification tasks, including the use of chromatography, filtration, and centrifugation techniques.</li>
<li>Prepare buffers, reagents, and media required for assays and cell culture work.</li>
<li>Analyze experimental data, maintain accurate lab records, and present findings in team meetings.</li>
<li>Collaborate with cross-functional team members to support the design, implementation, and optimization of research protocols.</li>
<li>Contribute to lab maintenance, including ordering supplies, organizing samples, and maintaining equipment.</li>
</ul>
Qualifications:
<ul>
<li>Education: Bachelor’s or Master’s degree in Molecular Biology, Biochemistry, Biotechnology, or a related field.</li>
<li>Experience: 1-3 years of hands-on experience in a research setting, preferably within a biotech or life sciences startup.</li>
<li>Technical Skills:
<ul>
<li>Proficiency in molecular biology techniques such as PCR, qPCR, cloning, and gel electrophoresis.</li>
<li>Experience with mammalian and/or bacterial cell culture, including cell line maintenance, transfection, and viability assays.</li>
<li>Knowledge of protein purification techniques (e.g., affinity, ion-exchange, size-exclusion chromatography) and experience using related equipment (e.g., AKTA).</li>
<li>Familiarity with assay development, including ELISA, reporter assays, and fluorescence-based assays.</li>
</ul>
</li>
<li>Computer Skills: Proficient in data analysis software (e.g., Excel, GraphPad Prism) and able to use standard lab information management systems.</li>
<li>Soft Skills: Strong attention to detail, excellent organizational skills, and the ability to work both independently and in a team.</li>
</ul>

Research Assistant

<h3>Job Description</h3>
Job DescriptionSalary: $19 - $23.57/hour 
Interested in Fishery Sustainability, Management and Hands on Marine Biology Work? Become a Marine Biologist!
 
A.I.S., Inc. (AIS) is a national scientific services firm supporting maritime activities requiring certification of compliance with environmental regulations as well as collecting data for use by Federal, State, Municipal, and other government agencies along the US coastline. AIS is looking forMarine Biologists(At-Sea Monitors)to work at sea collecting and recording data and biological samples for the National Marine Fisheries Service (NMFS) Northeast Fisheries Science Center (NEFCS) aboard commercial fishing vessels.
 
The primary goals of Northeast federal fishery observation programs are to provide quantitative biological, vessel, and gear-selectivity information for various New England and Mid-Atlantic fisheries. The At-Sea Monitor program focuses specifically on the groundfish industry, a grouping of fish that includes many commonly consumed fish such as cod, haddock and various flounder species. Each fishery observer or monitor operates on commercial fishing vessels operating in ports throughout New England and the Mid-Atlantic.If you ever wanted to make a difference, this is how.
 
Commercial fishing dates back hundreds of years. Today commercial fishing continues to be possible due to cooperation between fishermen and fisheries management scientists like yourself. In order to facilitate that cooperation, marine biologists collect data pertaining to fishing programs, economics, catch data, and fishing efficiency. Collected data is used to document stock information which is then used to protect the environment and preserve future generations of fish/fishermen. Commit to the journey!
 
Click to Learn More about Becoming a Fisheries Observer
 
At-Sea Monitors record detailed information on the gear and fishing activity of the vessels. Monitors work on deck on vessels ranging from 20 to 100 on trips roughly ranging from 1 to 14 days collecting data on fish catch and discard and incidental takes such as marine mammals, seabirds, and marine turtles. After attending a 3-week paid training in-person training inFalmouth, MAmonitors are deployed from ports throughout New England and Mid-Atlantic states. Gear types assessed include, trawl, gillnet, longline and handline.
 
Accommodations and meal reimbursement during in person session of training are provided.Training includes instructions on sampling protocols, gear, fisheries, fish identification, marine mammal/sea turtle identification, and safety.
 
This is a challenging job, and candidates must be mentally prepared to be away from home for multiple days, and must be physically able to handle heavy lifting, working odd hours, and long days in rough seas. Observing provides an excellent career in marine biology, as observers and monitors are widely recognized as being excellent field biologists. A broad range of advancement opportunities are available to those who demonstrate appropriate capabilities. Those opportunities include, but are not limited to, project management, field supervisors, and fieldwork in other programs.
 
Compensation:Monitorsstarting pay is $19.00/hour.Dependent on enrollment in our H&amp;W benefit, biologists may also be eligible for anadditional $4.57/hourfor the first 40 hours worked on each calendar week for a total of$23.57 hour. This is a fulltime position with benefits.Annually, monitors earn between $35K - $55K a yeardependent on their availability to deploy offshore and their personal sea day accomplishments. Monitors will be paid a minimum of 12 hours for each calendar day offshore and are also eligible for additional compensable activities while on land.
 
AIS benefits package includes health and dental insurance, vacation, sick and holiday benefits.Potential additional compensation consists of Data quality bonuses, Service awards, Fitness center reimbursement, Candidate Referral bonus.
 
Travel is reimbursedat an hourly rate along with compensation for miles accrued on a personal vehicle as well as per diem at the specified Government rate.
 
Minimum Qualifications:
<ul>
<li>High school diploma is required.</li>
<li>Experience with data entry on computers.</li>
<li>Monitor candidates must be U.S. citizens, or be legally authorized to work in the U.S.</li>
<li>Candidates must be physically able, as determined by a licensed physicians certification to perform observer duties.</li>
<li>Your own transportation is required.</li>
<li>Candidates are expected to commit to the program for at least one year.</li>
</ul>
 
Preferred Qualifications:
<ul>
<li>Bachelor's degree in biology or a related field from an accredited college or university with 30 credits of biology coursework, 6 credits of marine science is preferred.</li>
<li>At least one undergraduate course in math or statistics preferred.</li>
<li>At-sea experience</li>
<li>Coursework in Dichotomous Keys</li>
<li>Experience collecting Field Data and entering databases.</li>
</ul>
 
Locations:
<ul>
<li>Applicants must be currently living or be willing to live within 50 miles of Gloucester, Ma.</li>
</ul>
 
Contact:
If you would like to apply for one of these exciting new openings, please click the following link Careers Pageto submit the following information.
 
<ul>
<li>Resume</li>
<li>Cover Letter detailing sea and fish experience.</li>
<li>3 to 5 academic/professional references (name, email address and phone number)</li>
<li>Unofficial copies of your college (or high school if applicable) transcripts. </li>
</ul>
All documents must be submitted for your application to be considered. If you have any questions pertaining to this opening, please feel free to reach out to the Talent Team or 774-770-5833
 
An Equal Opportunity Employer
It is the policy of A.I.S. to recruit, hire, train, promote, transfer and compensate our employees and provide all other conditions of employment including Company sponsored events without regard to race, color, creed, religion, national origin, age, sex, gender identity, genetic information, marital status, lawful alien status, sexual orientation, physical or mental disability, citizenship status, veteran status or any other status protected by applicable law.
 
Must be able to work in the U.S. VEVRAA Federal Contractor Request Priority Protected Veteran Referrals Equal Opportunity Employer

Marine Biologist (ASM) - Gloucester, Ma

<h3>Job Description</h3>
Job Description
Team up with the most innovative company where Imagination becomes reality! E Ink is the originator, pioneer, and commercial leader in ePaper technology. The Billerica Research &amp; Development team is thriving and growing as we help develop products that are changing how people access information every day. We are seeking qualified candidates who are self-driven, looking to advance their career and become a high-impact player on a team.
Based on technology from MIT’s Media Lab, E Ink has transformed and defined the eReader market. Its Electrophoretic Display products make it the worldwide leader for ePaper. The Company’s corporate philosophy aims to deliver revolutionary products, user experiences and environmental benefits through advanced technology development.
Our diversity of people, backgrounds, experiences, thoughts and perspectives is fostered to create an inclusive work environment.
Our culture is built on value commitments to innovation, quality, results, integrity, community, people, and collaboration that foster a strong employee engagement, teamwork, safety and wellness.
We offer a competitive/generous benefits package that fits the needs of our employees. It includes health, dental, vision, wellness programs, employee discounts, 401k matches, ongoing development, advancement opportunities and more. This position is also eligible for our bonus program. (see E Ink │ Our Company)
About the position:
As a member of E Ink’s Process Development Team, the Senior Chemical Process Systems Engineer will be entrusted with fulfilling our mission of bringing smart displays to the world. This role is responsible for creating, improving, and maintaining pilot-scale systems that enable commercial-scale production of E Ink’s unique electrophoretic materials – including pigments, colloidal dispersions, microcapsules, and other additives.
We’re looking for someone who can help us build what we need, but also someone who can figure out what we should be building in the first place. This candidate will have experience designing and building specialized equipment and will be excited to drive equipment-based innovation across the organization!
Responsibilities
<ul>
<li>Design new process systems. Create PFDs, evaluate alternative technologies, generate P&amp;IDs, perform engineering calculations, draft fabrication drawings, work with outside vendors to select and customize process equipment, select components, and size lines</li>
<li>Lead the installation of new process systems in collaboration with both internal and external teams</li>
<li>Act as a companywide technical resource on process equipment such as reactor vessel design, pumps, mixers, temperature control systems, and sensors</li>
<li>Evaluate, select, and communicate with all relevant third-party vendors (piping, controls, etc.) required for the design and installation of new process equipment</li>
<li>Perform hands-on assembly, modification, commissioning, and troubleshooting of new and existing pilot-scale chemical process systems</li>
<li>Collaborate cross-functionally to coordinate capabilities within Development and Research departments, communicate support needs to Facilities department, and ensure responsiveness to EHS requirements</li>
</ul>
Qualifications
<ul>
<li>BS or MS in Chemical or Mechanical Engineering or equivalent work experience</li>
<li>7+ years of industrial process systems engineering experience</li>
<li>Ability to read P&amp;IDs, process flow diagrams, and fabrication drawings</li>
<li>Experience sizing and selecting chemical fluid lines, pumps, valves, and instrumentation</li>
<li>Basic electrical knowledge to read wiring diagrams and troubleshoot low voltage circuitry</li>
<li>Working knowledge of process automation (P&amp;ID controllers, instrumentation, transmitters, VFDs, PLCs)</li>
<li>Experience troubleshooting processes and equipment</li>
<li>Strong mechanical aptitude and hands-on attitude</li>
<li>Clear and effective communication skills</li>
<li>Ability to function effectively as a member of cross-functional, cross-disciplinary, and inter-corporate teams</li>
<li>Effective prioritization and time management to meet project goals / milestones</li>
</ul>
Preferred skills
<ul>
<li>Experience designing pressure vessels that comply with ASME BPVC</li>
<li>Experience commissioning new process equipment</li>
<li>Experience with mixer design</li>
<li>AutoCad proficiency</li>
<li>LabVIEW proficiency</li>
<li>Working knowledge of industrial codes (NFPA, NEC, ASME)</li>
<li>Basic SolidWorks and 3D printing skills</li>
<li>Experience operating machining equipment such as drill presses and lathes</li>
<li>Basic project management skills such as creating budgets, timelines, and updates on multiple small projects</li>
<li>Familiarity with Six Sigma / statistical analysis methods</li>
<li>Knowledge of typical fabrication methods</li>
</ul>
Benefits
<ul>
<li>Competitive total compensation package</li>
<li>Medical, dental and vision on 1st day</li>
<li>Company 401K match</li>
<li>20 PTO days</li>
<li>Generous sick leave policy</li>
<li>Casual day to day work environment</li>
<li>Hybrid/flexible work environment (for some positions)</li>
</ul>
E ink is committed to a diverse and inclusive workforce. E Ink is an equal opportunity employer and does not discriminate on the basis of race, ethnicity, gender, identity, sexual orientation, veteran’s status, disability, age, or on any basis prohibited by federal and state law.

746 Science Jobs